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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">KJIM</journal-id>
<journal-title-group>
<journal-title>The Korean Journal of Internal Medicine</journal-title><abbrev-journal-title>Korean J Intern Med</abbrev-journal-title></journal-title-group>
<issn pub-type="ppub">1226-3303</issn>
<issn pub-type="epub">2005-6648</issn>
<publisher>
<publisher-name>The Korean Association of Internal Medicine</publisher-name></publisher></journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3904/kjim.2019.430</article-id>
<article-id pub-id-type="publisher-id">kjim-2019-430</article-id>
<article-categories>
<subj-group>
<subject>Correspondence</subject></subj-group></article-categories>
<title-group>
<article-title>Response to comment on &#x0201c;Birt-Hogg-Dub&#x000e9; syndrome in Korean: clinicoradiologic features and long term follow-up&#x0201d;</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Lee</surname><given-names>Joo Hee</given-names></name>
<xref ref-type="aff" rid="af1-kjim-2019-430"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Jeon</surname><given-names>Min Joo</given-names></name>
<xref ref-type="aff" rid="af1-kjim-2019-430"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Song</surname><given-names>Joon Seon</given-names></name>
<xref ref-type="aff" rid="af2-kjim-2019-430"><sup>2</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Chae</surname><given-names>Eun Jin</given-names></name>
<xref ref-type="aff" rid="af3-kjim-2019-430"><sup>3</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Choi</surname><given-names>Jin-Ho</given-names></name>
<xref ref-type="aff" rid="af4-kjim-2019-430"><sup>4</sup></xref>
</contrib>
<contrib contrib-type="author">
<name><surname>Kim</surname><given-names>Gu-Hwan</given-names></name>
<xref ref-type="aff" rid="af5-kjim-2019-430"><sup>5</sup></xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">http://orcid.org/0000-0001-5121-3522</contrib-id>
<name><surname>Song</surname><given-names>Jin Woo</given-names></name>
<xref ref-type="corresp" rid="c1-kjim-2019-430"/>
<xref ref-type="aff" rid="af1-kjim-2019-430"><sup>1</sup></xref>
</contrib>
<aff id="af1-kjim-2019-430">
<label>1</label>Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, <country>Korea</country></aff>
<aff id="af2-kjim-2019-430">
<label>2</label>Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, <country>Korea</country></aff>
<aff id="af3-kjim-2019-430">
<label>3</label>Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, <country>Korea</country></aff>
<aff id="af4-kjim-2019-430">
<label>4</label>Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, <country>Korea</country></aff>
<aff id="af5-kjim-2019-430">
<label>5</label>Medical Genetics Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, <country>Korea</country></aff>
</contrib-group>
<author-notes>
<corresp id="c1-kjim-2019-430">Correspondence to Jin Woo Song, M.D. Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Korea Tel: +82-2-3010-3993 Fax: +82-2-3010-6968 E-mail: <email>jwsong@amc.seoul.kr</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>3</month>
<year>2020</year></pub-date>
<pub-date pub-type="epub">
<day>30</day>
<month>1</month>
<year>2020</year></pub-date>
<volume>35</volume>
<issue>2</issue>
<fpage>476</fpage>
<lpage>477</lpage>
<history>
<date date-type="received">
<day>17</day>
<month>12</month>
<year>2019</year></date>
<date date-type="accepted">
<day>20</day>
<month>12</month>
<year>2019</year></date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2020 The Korean Association of Internal Medicine</copyright-statement>
<copyright-year>2020</copyright-year>
<license>
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/">http://creativecommons.org/licenses/by-nc/4.0/</ext-link>) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions>
<related-article related-article-type="commentary-article" id="kjim-2019-430" elocation-id="kjim.2019.326"/>
</article-meta></front>
<body>
<p>Thank you for your interest in the article entitled &#x0201c;Birt-Hogg-Dub&#x000e9; syndrome in Korean: clinicoradiologic features and long term follow-up&#x0201d; and your comments. As you commented, we cited two papers as references that presented a lower incidence of skin lesions in Asian patients with Birt-HoggDub&#x000e9; (BHD) syndrome compared with Caucacian patients &#x0005b;<xref ref-type="bibr" rid="b1-kjim-2019-430">1</xref>,<xref ref-type="bibr" rid="b2-kjim-2019-430">2</xref>&#x0005d;.</p>
<p>In a study by Kunogi et al. &#x0005b;<xref ref-type="bibr" rid="b1-kjim-2019-430">1</xref>&#x0005d;, a folliculin (<italic>FLCN</italic>) germline mutation was found in 23 of the 36 patients by denaturing high performance liquid chromatography. The remaining 13 patients were examined by a real-time quantitative polymerase chain reaction, and a genomic deletion was found in two patients. Accordingly, an <italic>FLCN</italic> germline mutation was found in 25 of the 36 patients with multiple lung cysts. All patients were screened for skin lesion by dermatologists and skin lesions were detected in seven (28%) patients, and typical skin lesion (fibrofolliculoma) was confirmed in only one patient (4%) by skin biopsy. In another study by Furuya et al. &#x0005b;<xref ref-type="bibr" rid="b2-kjim-2019-430">2</xref>&#x0005d;, 76 of 156 <italic>FLCN</italic> mutation carriers (48.7%) had skin papules or tumors; however, typical fibrofolliculomas were confirmed in six (3.8%) by skin biopsy.</p>
<p>In Asian patients with BHD syndrome, low histologic confirmation rate may be due to inconspicuous skin lesions. In a study by Furuya et al. &#x0005b;<xref ref-type="bibr" rid="b2-kjim-2019-430">2</xref>&#x0005d;, with the exception of one individual, none of these patients cared or consulted dermatologists because skin manifestations were not their major complaint. Even though other biopsied papules macroscopically looked like fibrofolliculomas, histologic diagnosis varied and included perifollicular fibromas and sebaceous hyperplasia. Therefore, in the case of histologically unidentified skin lesions, the likelihood of fibrofolliculoma will be low. This also suggest that lung and kidney lesion may be more informative than fibrofolliculomas as diagnostic criteria for BHD syndrome in Asian populations &#x0005b;<xref ref-type="bibr" rid="b2-kjim-2019-430">2</xref>&#x0005d;.</p>
<p>Although one recent paper mentioned in the correspondence suggested a relatively higher incidence of skin lesions in Japanese patients with BHD syndrome &#x0005b;<xref ref-type="bibr" rid="b3-kjim-2019-430">3</xref>&#x0005d;, in addition to previous Japanese papers, recent papers including Korean and Chinese patients also suggested low incidence of typical skin lesions in Asian patients with BHD syndrome (20% in Korean and 7.4% in Chinese) &#x0005b;<xref ref-type="bibr" rid="b4-kjim-2019-430">4</xref>,<xref ref-type="bibr" rid="b5-kjim-2019-430">5</xref>&#x0005d;.</p>
<p>We appreciate your interests in our article and we hope that our explanation has addressed your questions.</p>
</body>
<back>
<fn-group>
<fn fn-type="conflict"><p>No potential conflict of interest relevant to this article was reported.</p></fn>
</fn-group>
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